WO2021123096A1 - Reactive phosporous contaning flame retardant and intrinsically flame retardant polymer obtainable by polycondensation with it - Google Patents

Reactive phosporous contaning flame retardant and intrinsically flame retardant polymer obtainable by polycondensation with it Download PDF

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Publication number
WO2021123096A1
WO2021123096A1 PCT/EP2020/086928 EP2020086928W WO2021123096A1 WO 2021123096 A1 WO2021123096 A1 WO 2021123096A1 EP 2020086928 W EP2020086928 W EP 2020086928W WO 2021123096 A1 WO2021123096 A1 WO 2021123096A1
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phosphorous containing
polymer
phosphorous
containing monomer
containing polymer
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PCT/EP2020/086928
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English (en)
French (fr)
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Thierry Badel
Delphine JOANNES
Sandra Chouzier
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Polytechnyl S.a.s.
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Priority to BR112022011818A priority Critical patent/BR112022011818A2/pt
Priority to US17/785,222 priority patent/US20230043028A1/en
Priority to CA3161803A priority patent/CA3161803A1/en
Publication of WO2021123096A1 publication Critical patent/WO2021123096A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
    • C07F9/6571—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms
    • C07F9/657163—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom
    • C07F9/657172—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus and oxygen atoms as the only ring hetero atoms the ring phosphorus atom being bound to at least one carbon atom the ring phosphorus atom and one oxygen atom being part of a (thio)phosphinic acid ester: (X = O, S)
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/02—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids
    • C08G69/26—Polyamides derived from amino-carboxylic acids or from polyamines and polycarboxylic acids derived from polyamines and polycarboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
    • C08G69/42—Polyamides containing atoms other than carbon, hydrogen, oxygen, and nitrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/02—Polyamides derived from omega-amino carboxylic acids or from lactams thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
    • C08L77/06—Polyamides derived from polyamines and polycarboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00—Properties
    • C08L2201/02—Flame or fire retardant/resistant
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00—Polymer mixtures characterised by other features
    • C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure

Definitions

  • the invention relates to a phosphorous containing monomer and a process thereof. Furthermore, the invention relates to a phosphorous containing polymer comprising said monomer and a production process thereof.
  • the phosphorous containing polymer of the invention is useful as flame-retardant polymer.
  • the invention relates to a thermoplastic polymer composition comprising said phosphorous containing polymer and optionally a further thermoplastic polymer.
  • the thermoplastic polymer composition can be used for the production of molded articles or yarns having excellent flame-retardant properties in order to ensure adequate fire protection.
  • Flame-retardant polymer compositions are useful for the production of molded articles in a large number of application fields because of their excellent property profile. In many applications, it is important that the polymer composition has excellent flame-retardant properties in order to ensure adequate fire protection. In addition, it is, however, also important that the further physical properties, such as e.g. tensile modus, tear strength and breaking elongation, fulfill the prescribed requirements for the respective application cases.
  • flame retardants are usually added to polymeric materials to enhance the flame-retardant properties of the polymers.
  • This approach provides high flexibility with regard to the polymeric materials although there are also limitations with respect to the required compatibility of the used flame retardant with the polymeric materials.
  • the flame retardants are subdivided in non-reactive and reactive flame retardants.
  • thermoplastic polymer compositions finished to be flame-retarding a large number of non-reactive flame-retardants has already been in technical use for a long time.
  • these are based in most cases on halogen- or antimony-containing substances which recently have come under public criticism due to their negative eco- and genotoxicologic potential.
  • halogen- and antimony-free non-reactive flame retardants are increasingly used, such as, e.g., red phosphor, melamine polyphosphate, melamine cyanurate or aluminum phosphinates, as are described in EP 1 070454 A.
  • the aforementioned flame retardants are only partly suitable for use in melt spinning processes employed for the production of polyamide or polyester fibers.
  • the halogenated flame retardants can considerably damage the spinning nozzle under the temperature and pressure conditions used during spinning.
  • melamine polyphosphate, melamine cyanurate or aluminum phosphinates are only insufficiently soluble in polyamides or polyesters, which results in an inhomogeneous distribution of the flame retardant in the base polymer. This leads to considerable drawbacks in particular in the melt-spinning process, since a clogging of the spinning nozzle is caused.
  • Another approach to provide a flame -retardant thermoplastic polymer composition is to use 9, lO-dihydro-9-oxa-lO-phosphaphenanthrene- 10-oxide (DOPO) based phosphorous flame-retardant polymers in said composition.
  • the 9, lO-dihydro-9-oxa-lO-phosphaphenanthrene- 10-oxide (DOPO) based phosphorous flame-retardant polymers are characterized in that certain monomers, in particular diacid monomers, are incorporated within the polymer backbone.
  • DOPO based flame-retardant polymers and production methods thereof are for example described in WO 2015/007783, CN 104231262 or CN 104211954. It is said that these halogen-free flame retardants are not toxic and can be processed easily together with thermoplastic molding compositions at high temperatures in a melt-spinning process or other extrusion processes.
  • the existing phosphorous containing flame retardant monomers based on DOPO are not able to bring high enough polyamide viscosity, which is necessary to carried out the spinning process in a satisfactory manner.
  • phosphorous-containing unsaturated polyesters comprising monomers derived from DOPO derivatives as described in the prior art, for example in WO 2013/139877 Al, are hardly suitable in melt- spinning or other extrusion processes together with a thermoplastic base polymer because the unsaturated carboxylic acid monomers in these unsaturated polyesters are unstable at higher temperatures.
  • flame-retardant monomers and polymers thereof with improved properties that can be used in different polymer substrates. It is particularly desirable to provide flame -retardant polymers exhibiting a high chemical stability and, if needed, a good solubility in thermoplastic base polymers which allows productions of, for example, fibers, molded articles or films from a composition comprising the flame-retardant polymer and optionally the thermoplastic base polymer at high temperatures, such as by melt spinning or other extrusion processes. Furthermore, it is desirable that the flame-retardant polymer can be distributed homogenously in the base polymer by a simple physical mixing under conditions, which are usual in a melt- spinning, extrusion or injection-molding process. The flame-retardant polymer should have low tendency to migrate out of the base polymer and, thus, produce a permanent flame-retarding effect.
  • a phosphorous containing monomer which is an adduct of a. 9, 10-dihydro-9-oxa-10-phosphaphenanthrene- 10-oxide (DOPO) and/or a nuclear substituted DOPO derivative with b. at least one unsaturated divalent carboxylic acid, ester or anhydride thereof, as defined in formula (I) or (II)
  • Ri is a linear chain containing at least 4 carbon atoms and at least one double bond
  • R2 and R3 are independently hydrogen, an alkyl group or an aryl group.
  • the phosphorous containing monomer of the invention differs from the phosphorous containing monomers known in the prior art in that the phosphor atom of DOPO and it derivatives is directly bounded to a carbon atom of the linear chain (Rl) of the divalent carboxylic acid, ester or anhydride thereof, as defined in formula (I) or (II). Additionally, according to the invention, said linear chain contains at least 4 carbon atoms.
  • Rl the linear chain contains at least 4 carbon atoms.
  • Another aspect of the invention relates to a production method of said monomer, wherein in a first process step the unsaturated divalent carboxylic acid, ester or anhydride thereof is produced by catalytic dimerization of a carboxylic acid or ester according to formula (III) or (Ilia) or a mixture thereof (III) (Ilia), wherein,
  • R4 and R4 a are independently a linear chain containing at least 2 carbon atoms and at least one double bond and R2 and R3 are independently hydrogen, an alkyl group or an aryl group, and in a further process step 9,10-dihydro-9-oxa-10-phosphaphenanthrene-
  • DOPO 10-oxide
  • nuclear substituted DOPO derivative is added to the obtained unsaturated divalent carboxylic acid, ester or anhydride thereof.
  • the present invention relates to phosphorous containing polymer and production process thereof, which is useful as flame retardant polymer and obtainable by polycondensation of at least one phosphorous containing monomer according to the invention, at least one diamine, diol, aminoacid, lactam, hydroxycarboxylic acid or lactone and optionally another monomer.
  • another aspect of the present invention relates to a thermoplastic polymer composition comprising at least one of the above flame-retardant polymer and optionally a further thermoplastic polymer.
  • thermoplastic polymer shall mean a polymer that becomes pliable or moldable above a specific temperature, so is capable of flow at high temperatures below the thermal decomposition temperature and returns to a solid state upon cooling.
  • a polymer is a macromolecular compound prepared by reacting (i.e., polymerizing, condensation) monomers of the same or different type, including homo- and copolymers.
  • Thermoplastic materials are made by chain polymerization, polyaddition and / or polycondensation.
  • a range of values for a variable defined by a bottom limit, or a top limit, or by a bottom limit and a top limit, also comprises the embodiments in which the variable is chosen, respectively, within the value range: excluding the bottom limit, or excluding the top limit, or excluding the bottom limit and the top limit.
  • the description of several successive ranges of values for the same variable also comprises the description of embodiments where the variable is chosen in any other intermediate range included in the successive ranges.
  • the present description also describes the embodiment where: “the magnitude X is at least 11", or also the embodiment where: “the magnitude X is at least 13.74", etc.; 11 or 13.74 being values included between 10 and 15.
  • a plurality of elements includes two or more elements.
  • a and/or B refers to the following selections: element A; or element B; or combination of elements A and B (A+B).
  • the phrase ‘A and/or B’ is equivalent to at least one of A and B.
  • the phrase ‘A and/or B’ equates to at least one of A and B .
  • the phrase ‘Al, A2, and/or A3’ refers to the following choices: Al; A2; A3; A1+A2; A1+A3; A2+A3; or A1+A2+A3.
  • a multivalent alcohol denotes one multivalent alcohol or more than one multivalent alcohol.
  • One aspect of the present invention relates to a phosphorous containing monomer, which is an adduct of a. 9, 10-dihydro-9-oxa-10-phosphaphenanthrene- 10-oxide (DOPO) and/or a nuclear substituted DOPO derivative with b. at least one unsaturated divalent carboxylic acid, ester or anhydride thereof, as defined in formula (I) or (II)
  • Ri is a linear chain containing at least 4 carbon atoms and least one double bond
  • R2 and R3 are independently hydrogen, an alkyl group or an aryl group.
  • DOPO has the following chemical structure:
  • Nuclear substituted DOPO derivatives denotes DOPO derivatives which are for example described in WO 2019/081226 and bear one or more substituents on the aromatic rings of DOPO. Each ring may bear 0 to 4 substituents, which can for example be selected from alkyl, alkoxy, aryl, aryloxy and aralkyl.
  • the alkyl moiety in alkyl, alkoxy and aralkyl may have, for example, 1 to 30 carbon atoms, which may be linear, branched or cyclic and which may be saturated or unsaturated, preferably saturated.
  • the aryl in aryl, aryloxy and arylalkyl may, for example, comprise 6 to 30 carbon atoms, such as phenyl and naphthyl. If the DOPO molecule bears more than one nuclear substituent, these substituents may be identical or different to each other.
  • Linear chain means that all the carbon atoms of the chain backbone are linked to 1 or 2 carbon atoms. As opposed to a “branched chain”, in which at least one carbon atom of the chain backbone is linked to more than two carbon atoms.
  • the linear chain (Ri) of the unsaturated divalent carboxylic acid, ester or anhydride thereof, as defined in formula (I) or (II), contains at least 4 carbon atoms, preferably 4 to 10 carbon atoms, more preferably 4 to 8 carbon atoms, most preferably 4 carbon atoms. Additionally, the linear chain (Ri) contains at least one double bound, preferably at least 2 or at least three double bounds. In a preferred embodiment of the invention the linear chain (Ri) contains one double bound.
  • the linear chain Ri of formula (I) or (II) is 1 -butylene or 2-butylene.
  • the substituents R2 and R3 of the unsaturated divalent carboxylic acid, ester or anhydride thereof, as defined in formula (I) or (II), are hydrogen, alkyl or aryl groups.
  • the R2 and R3 are independently selected from linear, branched and/or cyclic Ci- 6 alkyl residues or C6-18 aryl residues, for example methyl, ethyl, propyl, isopropyl, butyl, tert.-butyl, cyclohexyl, phenyl or naphthyl. More preferred R2 and R3 are independently selected from hydrogen, ethyl or methyl.
  • the phosphorous containing monomer has the following formula (IV)
  • R2 and R3 are preferably hydrogen, ethyl or methyl.
  • the phosphorous containing monomer as described above is produced such that in a first process step the unsaturated divalent carboxylic acid, ester or anhydride thereof, as defined in formula (I) or (II), is produced by catalytic dimerization of a carboxylic acid or ester according to formula (III) or (Ilia) or a mixture thereof
  • R4 and R4 a are independently a linear chain containing at least 2 carbon atoms and at least one double bond and R2 and R3 are independently hydrogen, an alkyl group or an aryl group as defined above.
  • R4 and R4 a are independently a linear chain containing 2 to 5, more preferably 2 to 4 carbon.
  • linear chains R4 and R4 a contain at least one double bound, preferably independently from each other at least two, at least three double bounds. In a preferred embodiment R4 and/or R4 a contain one double bound. In a further preferred embodiment, R4 and R4 a are identical. In a most preferred embodiment, R4 and/or R4 a are ethylene.
  • the catalytic dimerization is carried out under common dimerization reaction conditions, wherein the catalyst preferably is selected from the group consisting of alkyl phosphinite, aryl phosphinite, alkyl phosphinate, aryl phosphinate, metallic catalysts, which are selected from the group consisting of Ni, Pd, Ru, Rh, and mixtures thereof. Suitable metal catalysts are for example described in US 4,638,084 or US 4,889,949.
  • the catalytic dimerization reaction is carried out at a temperature between 80 and 200 °C, more preferably between 100 and 150 °C for a period of 2 to 6 hours , more preferably of 3 to 5 hours.
  • the produced unsaturated divalent carboxylic acid, ester or anhydride thereof reacts further with 9,10-dihydro-9-oxa-10- phosphaphenanthrene- 10-oxide (DOPO) and/or nuclear substituted DOPO derivative as defined above.
  • DOPO 9,10-dihydro-9-oxa-10- phosphaphenanthrene- 10-oxide
  • the DOPO and/or nuclear substituted DOPO derivative may directly added to (mixed with) the unsaturated divalent carboxylic acid, ester or anhydride thereof obtained in the first process step or after isolation and purification of the unsaturated divalent carboxylic acid, ester or anhydride thereof.
  • common isolation and purification methods as known in the art are suitable.
  • the formation of the adduct of DOPO and/or nuclear substituted DOPO with the unsaturated divalent carboxylic acid, ester or anhydride thereof as described above, i.e. the formation of the phosphorous containing monomer of the invention is carried out at a temperature between 80 to 120 °C, more preferably between 90 and 110 °C, for a period of 40 to 70 hours, more preferably for a period of 45 to 60 hours.
  • the obtained adduct according to the invention can be easily purified by using method as known the art.
  • the purity of the phosphorous containing monomer of the invention is preferably at least 95 % or more, more preferably at least 98 % or more.
  • the product yield is preferably between 70 and 90 %, preferably between 75 and 85%.
  • the phosphorous containing monomer of the invention is an ester
  • the corresponding acid may obtained by saponification and/or hydrolysis of the ester under common reaction conditions.
  • the phosphorous containing monomer of the invention may be used to produce a phosphorous containing polymer having good flame-retardant properties, i.e. to produce flame retardant thermoplastic polymers.
  • the phosphorous containing polymer is obtainable by polycondensation of a. at least one phosphorous containing monomer according to the invention, b. at least one monomer selected from the group consisting of diamine, diol, aminoacid, lactam, hydroxycarboxylic acid, lactone and mixtures thereof, and c. optionally other monomers.
  • the phosphorous containing polymer of the invention may be a homo- or a copolymer.
  • the phosphorous containing homopolymer of the invention comprises the phosphorous containing monomer of the invention and one diamine, diol, aminoacid, lactam, hydroxycarboxylic acid or lactone monomers as defined below.
  • the phosphorous containing copolymer of the invention comprises the phosphorous containing monomer of the invention and different diamine, diol, aminoacid, lactam, hydroxycarboxylic acid and/or lactone monomers, and optionally other monomers, as defined below.
  • the phosphorous containing polymer is halogen-free.
  • the phosphorous containing polymer of the invention has a phosphorous content of at least 0.1 % by weight.
  • the phosphorous content is given in % by weight based on the total weight of the polymer.
  • the polymer has a phosphorous content of at least 0.5 % by weight, more preferably at least 0.9 % by weight.
  • the upper limit of the phosphorous content in the polymer of the invention is not particularly limited. Generally, the phosphorous content should not be above 15 % by weight, preferably at a maximum of 10 % by weight, more preferably at a maximum of 9% by weight and even more preferably at a maximum of 8 % by weight.
  • the given lower and upper limits of the phosphorous content can be combined with each other. Suitable ranges are, for example, at least 0.1 % to about 15 % by weight and about 0.5 % to about 9 % by weight. Other combinations of lower and upper limits are possible as well.
  • the phosphorous content is about 0.5 % to about 15 % by weight, more preferably about 0.9 % to about 10 % by weight, even more preferably about 0.9 % to about 8.5 % by weight, most preferably about 0.5 to about 5 % by weight, each of the total weight of the polymer.
  • the phosphorous-containing monomer of the invention does not contain any carbon carbon double bonds except aromatic bonds.
  • the phosphorous containing polymer of the invention may be obtained by polycondensation of the phosphorous containing monomer of the invention with at least one monomer selected from the group consisting of diamine, diol, amino acid, lactam, hydroxycarboxylic acid, lactone or mixture thereof as further specified below.
  • the diamine used in the invention may contain primary, secondary or secondary and one or more tertiary amine groups.
  • the diamine is an alkane diamine of 4 to 12 carbon atoms or a solution of a salt of an alkanedicarboxylic acid of 4 to 12 carbon atoms and an alkane diamine of 4 to 12 carbon atoms or mixtures thereof.
  • the alkane diamine used in the present invention may be a linear, branched, cycloalkane, heterocycloalkane diamine or phenylalkyldiamine.
  • phenylalkyl diamines are m-xylylenediamine or p- xylylenediamine.
  • the diamine is selected from the group consisting of 1,6-hexanediamine, 1,8-octadiamine, 1,10-decanediamine, 1,12-docdecanediamine, hexamethylenediamine (HMD), heptamethylene diamine, tetramethylene diamine, octamethylene diamine, nonamethylene diamine, decamethylene diamine, 2-methylpenta-methylene diamine, undecamethylene diamine, dodecamethylene diamine, isophorone diamine, 1,4- diaminobutane, 1,5-diaminopentane, 1,9-diaminononane, 4,4- diaminodicyclohexylmethane (PACM), or mixtures thereof.
  • HMD hexamethylenediamine
  • heptamethylene diamine heptamethylene diamine
  • tetramethylene diamine tetramethylene diamine
  • octamethylene diamine nonamethylene diamine
  • the diamine is HMD.
  • the alkanedicarboxylic acid used in the present invention may be a linear, branched, cycloalkane or heterocycloalkane dicarboxylic acid. More preferably, the alkanedicarboxylic acid is selected from the group consisting of adipic acid, suberic acid, sebacic acid, dodecanedioic acid, isophthalic acid, terephthalic acid, azelaic acid, pimelic acid, naphthalene dicarboxylic acid or mixtures thereof. According to the invention, adipic acid is the preferred and most used monomer.
  • Suitable secondary diamines which may contain also one of more tertiary amine groups, are described for example in WO 2019/081226 Al.
  • the diol used in the present invention is selected from the group consisting of alkane diols, glycols, phosphine oxides or mixtures thereof.
  • the alkane diol may be a linear, branched, cycloalkane or heterocycloalkane.
  • the alkane diols contains 2 to 30 carbon atoms, preferably 2 to 20 carbon atoms, more preferably 2 to 15 carbon atoms, even more preferred 2 to 12 carbon atoms.
  • diols examples include 1,2-propandiol, 1,3-propandiol, 1,3-butandiol, 1,4-butandiol, 2,3-butandiol, ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, neopentylglycol, diethyl glycol, isosorbide, cyclohexanedimethanol, tricyclodecan-dimethanol, bispropoxylate Bisphenol A, hydrogenated bisphenol A phosphine oxides as described in WO2018/197173 Al or mixtures thereof.
  • Suitable aminoacids and lactams according to the invention are for example amino-caproic acid, epsilon-caprolactam, 12-aminododecanoic acid, laurolactam, 11-aminoundecanoic acid or 10-aminodecanoic acid.
  • the lactam is epsilon-caprolactam.
  • Suitable hydroxycarboxylic acids and lactone according to the invention are for example lactic acid, glycolic acid, caprolactone and malic acid.
  • the above described phosphorous containing polymer may optionally comprise other monomers in addition to the first phosphorous -containing monomer of the invention. These other monomers are not particularly limited as long as they can react with the phosphorous containing monomer of the invention or the diamine, diol, lactam, aminoacid, hydroxycarboxylic acid or lactone as described above to form the polymer.
  • the other monomer does not contain any carbon carbon double or triple bond except aromatic bonds in order to obtain a final flame-retardant polymer of high thermal stability.
  • the "other monomers” can be selected or example from di- and multivalent carboxylic acids and di- or multivalent amines, which may or may not comprise phosphorous atoms or other heteroatoms, such as oxygen, nitrogen and sulfur.
  • Other monomers which can for example form block copolymers with the polyamide units of monomer of the invention and the diamine, may be used.
  • “other monomers” c) can, for example, be selected from carboxyphosphinic acid derivatives, such as carboxyethyl-phenylphosphinic acid (CEPPA) and carboxyethyl-methylphosphinic acid (CEMPA), aminophosphinic acid derivatives making an amide bond by polycondensation, such as aminomethyl phosphinic acid (AMPA), biscarboxyphosphine oxide derivatives, such as bis(beta-carboxyethyl)methylphosphine oxide (CEMPO), bisaminophosphine oxide derivatives making an amide bond by polycondensation, such as bis(3-aminopropyl)methylphosphine oxide (AMPO), aliphatic diols, such as monoethylene glycol, diethylene glycol, propylene glycol, 1,3-propanediol, 1,3-butandiol, 1,4-butandiol, neopenthyl glycol,
  • the phosphorous containing polymer according to the invention can be end-capped by reaction with a monovalent amine and/or monovalent alcohol and/or a monovalent carboxylic acid as known in the art.
  • the chemical and physical properties of the polymer according to the invention can be influenced by selecting the other monomers such that these monomers are di- or multivalent monomers. If only divalent monomers are employed, no cross-linking between the polymer backbones occurs. If multivalent monomers are used, cross-linking could occur. By selecting a suitable ratio between di- and multivalent monomers, the degree of cross-linking and thus the properties of the polymer can be tailored.
  • the phosphorous containing polymer may have an average molecular weight Mn of above 1,000 g/mol, preferably of above 3,000 g/mol, of above 5,000 g/mol or even more preferably of above 6,500 g/mol, most preferably between 5,000 and 8,000 g/mol.
  • the average degree of polymerization of the phosphorous containing polymer preferably amounts to, at least 5, preferably at least 15, even preferably at least 25.
  • the phosphorous containing polymer of the invention has a high phosphorous content of at least 4.0 % by weight, based on the total weight of the phosphorous containing polymer.
  • the polymer has a phosphorous content of at least 5.0 % by weight, more preferably at least 5.8 % by weight, even more preferably at least 7.0 % by weight, such as at least 7.5 % by weight.
  • the upper limit of the phosphorous content of the polymer of the invention is not particularly limited. Generally, the phosphorous content is preferably 15 % by weight or lower, preferably 10 % by weight or lower, more preferably 9% by weight or lower and even more preferably 8 % by weight or lower.
  • the given lower and upper limits of the phosphorous content can be combined with each other. Suitable ranges are, for example, at least 4.0 % to about 15 % by weight and about 5.0 % to about 9 % by weight.
  • the phosphorous content is about 5.0 % to about 15 % by weight, more preferably about 5.8 % to about 10 % by weight, even more preferably about 7.0 % to about 9 % by weight, and most preferably about 7.5 % to about 8.5 % by weight, each of the total weight of the monomer.
  • the average molecular weight Mn of the polymer according to the invention is above 8,000 g/mol, preferably above 10,000 g/mol, above 15,000 g/mol or even more preferably above 16,000 g/mol, most preferably between 8,000 and 20,000 g/mol.
  • the average degree of polymerization of the phosphorous containing polymer preferably amounts to at least 80, preferably to at least 100, even more preferably to at least 130, most preferably between 80 and 165. Additionally, in this embodiment of the invention it is preferred that the phosphorous containing polymer of the invention has a low phosphorous content preferably between 0.1 and 3.0 % by weight, more preferably between 0.25 and 2.0 % by weight, most preferably between 0.5 and 1.0 % by weight, based on the total weight of the phosphorous containing polymer.
  • the viscosity of the polymer of the invention is closed to the one of the corresponding polymer not containing the phosphorous comonomer of the invention .
  • an optimum processability and property of the polyamide of the invention in the melt-spinning process and other extrusion processes are obtained.
  • the desired viscosity can be further adjusted by an accurate monitoring of the average molecular weight Mn, the average degree of polymerization DPn and/or the degree of branching of the polymer of the invention.
  • the phosphorous containing polymer of the invention shows good flame-retardant properties.
  • the chemical and physical properties of the phosphorous containing polymer according to the invention can further be influenced by the temperature and time of polycondensation, solid-state postcondensation, the catalyst used and the addition of, for example, chain prolongation and chain branching monomers.
  • Heat stabilizers may also be added.
  • To improve the color of the flame-retardant polymer according to the invention it is further possible to use known optical brightening agents.
  • a further embodiment of the present invention relates to a process of preparing the above described phosphorous containing polymer.
  • This process comprises the steps of a) reacting 9, 10-dihydro-9-oxa-10-phosphaphenanthrene- 10-oxide (DOPO) and/or nuclear substituted derivatives thereof with at least one unsaturated divalent carboxylic acid, ester or anhydride thereof, as defined in formula (I) or (II), to obtain a phosphorous -containing monomer of the invention; b) reacting the phosphorous-containing monomer obtained in step a) with at least one one monomer selected from the group consisting of diamine, diol, aminoacid, lactam, hydroxycarboxylic acid, lactone or mixtures thereof as described above; and c) optionally carrying out the reaction in step b) in the presence of at least one other monomer, and/or optionally carrying out the reaction in step b) in the presence of at least one monovalent carboxylic acid and/or monovalent amine and
  • thermoplastic polymer composition comprising the phosphorous containing polymer according to the invention mainly or even only or in combination with another thermoplastic polymer to impart flame-retardant properties of that thermoplastic polymer. Therefore, in a further embodiment, the present invention relates to a thermoplastic polymer composition comprising at least one phosphorous containing polymer as described above and optionally a thermoplastic polymer.
  • thermoplastic polymer optionally used in the thermoplastic polymer composition of the invention can be selected from a broad variety of polymers, in particular synthetic polymers, including homopolymers, copolymers and block copolymers. Also mixtures of one or more thermoplastic polymers may be used.
  • a list of suitable synthetic polymers is, for example, disclosed in WO 2008/119693 Al, the content of which is incorporated herein by reference.
  • thermoplastic polymers are, for example, polyamides, polyphthalamides, polyesters including unsaturated polyester resins, polysulfones, polyimides, polyolefins, polyacrylates, polyether etherketones, acrylonitril butadiene styrenes (ABS), polyurethanes, polystyrenes, polycarbonates, polyphenylene oxides, phenolic resins and mixtures thereof.
  • the thermoplastic polymer is a polyamide, such as a polyamide that is suitable for melt spinning or other molding processes.
  • the polyamide can, for example, be selected from the group consisting of PA 6.6, PA 6, PA 6.10, PA 6.12, PA MXD.6, PA 11 and PA 12.
  • Copolyamides, such as PA 6.6/6 and PA 6.6/6.T and blends of polyamides, such as PA 6.6/PA 6 and PA 6.6/PA 6.10 are suitable as well.
  • the amount of flame-retardant polymer in the thermoplastic polymer composition according to the invention is not particularly limited and can be selected by a person skilled in the art according to the requirements.
  • the thermoplastic polymer composition comprises the phosphorous containing polymer, i.e. the flame -retardant polymer, of the invention in an amount of at least 80 % by weight, preferably of at least 85 % by weight, or of at least 90 % by weight, more preferably of at least 95 % by weight, even more preferably of at least 98 % by weight, most preferably of at least 99 % by weight, based on the total weight of the thermoplastic composition.
  • the phosphorous containing polymer is a copolymer.
  • the thermoplastic polymer composition comprises at least 0.1 % by weight, preferably at least 2 % by weight of the phosphorous containing polymer of the invention based on the total weight of the thermoplastic polymer composition.
  • the thermoplastic polymer composition can comprise from about 0.1 % to about 30 % by weight, preferably from about 2 % to about 25 % by weight, even more preferably from about 5 % to about 20 % by weight of the phosphorous containing polymer, based on the total weight of the thermoplastic polymer composition.
  • the thermoplastic polymer composition of the invention comprise the phosphorous containing polymer in an amount such that the final thermoplastic polymer composition has a phosphorous content of from about 0.1 % to about 5 % by weight, preferably of from about 0.1 % to about 2 % by weight, in particular of from about 0.5 % to about 1 % by weight, based on the total weight of the thermoplastic polymer composition.
  • thermoplastic polymer composition containing a higher phosphorous content of up to, for example, about 5 % by weight of the total weight of the composition and then add this master batch to another thermoplastic polymer composition for tailoring its properties.
  • the viscosity of the final thermoplastic polymer composition of the invention is closed to the one of thermoplastic polymer compositions known in the art, which do not contain the phosphorous comonomer of the invention.
  • an optimum processability and property of the composition of the invention in the melt-spinning process and other extrusion processes are obtained.
  • the desired viscosity can be further adjusted by an accurate monitoring of the average molecular weight Mn, the average degree of polymerization DPn and/or the degree of branching of the polymer of the invention.
  • the final thermoplastic polymer composition of the invention has a viscosity number of 80 to 250 ml/g, more preferred of 100 to 180 ml/g, even more preferred of 110 to 140 ml/g, measured in solution according to ISO307 standard.
  • These viscosity number ranges correspond to the viscosity number ranges of the aliphatic polyamide compositions such as PA66, PA6 and PA610.
  • the melt viscosity of final thermoplastic polymer composition of the invention is preferably of 50 to 300 Pa ⁇ s, more preferably of 70 to 250 Pa ⁇ s, even more preferably of 100 to 200 Pa ⁇ s, measured by a rheometer with a cone-plate geometry at a temperature ranging from 25 to 30 °C above the melting point of the thermoplastic polymer composition under a stepwise shear sweep ranging from 1 to 160 s 1 .
  • thermoplastic composition can be used to produce flame-retardant polymer fibers.
  • the thermoplastic composition of the invention which comprises mainly or even only the phosphorous containing polymer of the invention, is directly spun to form filaments.
  • the phosphorous-containing polymer has a phosphorous content from about 0.1 to about 2 % by weight, preferably from 0.1 to 1 % by weight, even more preferred from 0.1 to 0.5 % by weight, based on the total weight of the phosphorous containing polymer.
  • the phosphorous containing polymer of the invention is physically mixed with another appropriate thermoplastic polymer, such as for example a polyamide, in the melt, and the mixture is then either directly spun as a polymer mixture having a phosphorous content of between about 0.1 % and about 1 % by weight, so as to form filaments, or, the mixture is then tailored in terms of a master batch having a phosphorous content of between about 2 % and about 5 % by weight, and is then added to the same or a different type of polyamide and spun to filaments in a second process step.
  • another appropriate thermoplastic polymer such as for example a polyamide
  • Polymer fibers produced in a melt-spinning process from a thermoplastic polymer composition of the present invention preferably have a total phosphorous content of from about 0.1 % to about 2 % by weight, in particular of from about 0.5 to about 1 % by weight, based on the total weight of the thermoplastic polymer composition, and they are therefore sufficiently flame proof. All aforementioned polymers can be finished in an excellent manner to be flame-retarding with the aforementioned phosphorous containing polymer by a simple physical mixing of the polymer melts under conditions as are usual in the melt-spinning process. When using the phosphorous containing polymer according to the invention, important polymer properties, such as the melt viscosity, the melting point of the polymer composition obtained after mixing are changed only to an extent that a reliable processing, such as a melt spinning remains entirely ensured.
  • thermoplastic polymer composition of the present invention may additionally comprise other flame retardants or additives known to a person skilled in the art, in particular those flame retardants and additives which are used in the preparation of fibers.
  • Suitable other flame-retardants are, for example, melamine cyanurate, melamine polyphosphate, ammonium polyphosphate and metal stannates, preferably zinc stannate, metal borates such as zinc borate, polyhedral oligomeric silsesquioxanes (for example trade name POSS of Hybrid Plastics), and so-called nanoclays based on the exfoliated phyllosilicates montmorillonite and bentonite, such as, e.g., the products Nanomer of Nanocor, or Nanofil of Sudchemie, and inorganic metal hydroxides such as the products Magnifin or Martinal of Martinswerk.
  • parameters that are important to the flame-retarding properties can be modified, for example the characteristic cone calorimetric numbers TTI (time to ignition) can be increased, PHRR (peak of heat release rate) can be reduced and/or a desired suppression of the smoke gas generation can be improved.
  • TTI time to ignition
  • PHRR peak of heat release rate
  • both, the phosphorous containing polymer as well as the thermoplastic polymer composition according to the invention may comprise additional components, such as anti-dripping agents, polymer stabilizers, anti-oxidants, light stabilizers, peroxide scavengers, nucleating agents, fillers and reinforcing agents, and other additives, such as blend compatibilizing agents, plasticizers, lubricants, emulsifiers, pigments, rheology additives, catalysts, flow-control agents, optical brighteners, flame-proving agents, antistatic agents and blowing agents. Specific examples of these additives are disclosed in
  • Viscosity Number (unit: mL/g) was determined in solution in formic acid according to ISO307 standard.
  • Melt viscosity was measured by a rheometer with a cone-plate geometry, at 280°C.
  • Carboxylic acid End-Groups (CEG) concentration and Amine End-Groups (AEG) concentration were determined by potentiometric titration (unit: meq/kg).
  • Adipic acid, hexamethylenediamine and hexamethylenediammonium adipate from Solvay Adipic acid, hexamethylenediamine and hexamethylenediammonium adipate from Solvay.
  • Ukanol FR80 from Schill Seilacher, containing 8.0%w of phosphorus according to technical data sheet.
  • Ukanol FR 80 is used in US 2013/0136911 A1 as flame retardant.
  • Methyl acrylate (type III), palladium acetylacetonate (0.3 mmol per mol of methylacrylate), tri-tert-butylphosphonium tetrafluoroborate (31.5 mmol per mol of methylacrylate) and tetrafluoroboric acid (12.6 mmol per mol of methylacrylate) were poured in a stainless steel reactor. The temperature was increased to 110°C and kept 4h. After extraction and purification, dimethyl hex- 2-endioate was obtained. Syntheses of phosphorous containing monomer (IV)
  • the phosphorylated dicarboxylic acid was then obtained by saponification and/or hydrolysis of the corresponding phosphorylated diester obtained in previous examples 2. 4. lg (2.57 mmol) of unsaturated methyl ester (I) and 0.27g (11 mmol) of LiOH was dissolved in a water/THF mixture (50/50 wt.- %). The reaction mixture was kept at 30°C for 2h. The reaction mixture is then acidified with HC1.
  • the phosphorous containing monomer has the following structure: Synthesis of copolymers
  • the polyamide had a melting point of 254 °C, a crystallization temperature of 207°C, and a thermal degradation onset of 391°C, and a char at 500°C of 8%.
  • the viscosity number was 140 mL/g.
  • the melt viscosity at 280°C under 100s- 1 was 160 Pa.s.
  • the phosphorous content was 0.5 %w.
  • the carboxylic end group is 73 meq/kg, and the amino end group is 31 meq/kg ; the estimated molecular weight is 19000g/mol, corresponding to a degree of polymerization (DPn) of about 164.
  • Example 5 130.0 g (0.50 mol) of hexamethylenediammonium adipate, 16.31 g (0.04 mol) of phosphorous containing monomer from Example 2 and 15.15 g (0.04 mol) of hexamethylenediamine 32.2% aqueous solution were poured with 129.0 g of demineralized water and antifoam in a stainless steel clave equipped with a mechanical stirrer with an internal thermometer. The clave atmosphere was purged with nitrogen, and the temperature was increased progressively to 220°C, with continuous stirring, letting pressure increase up to about 17.5 bar. The temperature was increased progressively up to 250°C, while maintaining the same level of pressure.
  • the polyamide had a melting point of 245 °C, a crystallization temperature of 193°C, and a thermal degradation onset of 382°C, and a char at 500°C of 10%.
  • the viscosity number was 129 mL/g.
  • 100s- 1 was 130 Pa.s.
  • the phosphorous content was 0.9 %w.
  • the carboxylic end group is 72 meq/kg, and the amino end group is 30 meq/kg ; the estimated molecular weight is 19500g/mol, corresponding to a degree of polymerization (DPn) of about 161.
  • a semi crystalline polymer was obtained with the following analytical data:
  • the polyamide had a melting point of 261 °C, a crystallization temperature of 225°C, and a thermal degradation onset of 423 °C, and a char at 500°C of 7%.
  • the viscosity number was 131 mL/g.
  • the melt viscosity at 280°C under lOOs-1 was 150 Pa.s.
  • the carboxylic end group is 88 meq/kg, and the amino end group is 40 meq/kg ; the estimated molecular weight is 15600g/mol, corresponding to a degree of polymerization (DPn) of about 138.
  • the polyamide had a melting point of 257°C, a crystallization temperature of 221 °C, and a thermal degradation onset of 374°C, and a char at 500°C of 10%.
  • the viscosity number was 37 mL/g.
  • the melt viscosity at 280°C under 100s- 1 was 1 Pa.s.
  • the phosphorous content was 0.9 %w.
  • the Examples 4 and 5, according to the invention, enable to prepare phosphorous containing polyamides with appropriate viscosity number and melt viscosity, similar to those of the PA66 (CE1), whereas the phosphorous containing monomer of CE2 prevents to reach high enough viscosity number and melt viscosity.
  • Example 7 shows that the homopolymerization of the phosphorous containing monomer from Example 2 is possible, whereas the phosphorous containing monomer of CE3 prevents to do so.
  • the PA66 pellets (Stabamid 26AE1) were dried at 90 degrees centigrade in a vacuum oven for one night. A 10 g dry blend was then prepared with PA66 and the phosphorous containing polymer of Example 7, with the corresponding ratio 92.4%/7.6% by weight for approx. 0.5% weight of phosphorous in the final composition.
  • the production of the melt blend was effected by melt blending with a twin screw microcompounder Xplore, equipped with a recycling channel and a water cooling bath. The time of melt blending prior to extrusion was set to 9 minutes, and the melt temperature of the mass was 280°C. After melt-blending, the viscosity number was 137 mL/g.
  • the limiting oxygen index (LOI) test was carried out according to the ISO 4589-2 standard on the compression molded bars (100 mm x 6.5 mm x 3 mm) using the top surface ignition method.
  • the combustibility of the materials was determined by cone calorimeter according to the ISO 5660-1 standard, on the compression molded plates (100 mm x 100 mm x 3 mm), using a heat flux of 35 kW/m 2 .
  • TTI stands for time to ignition, THR for total heat release, pHRR for peak heat release rate, and TSR for total smoke released.
  • Table 1 Flame retardant properties.

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PCT/EP2020/086928 2019-12-20 2020-12-18 Reactive phosporous contaning flame retardant and intrinsically flame retardant polymer obtainable by polycondensation with it WO2021123096A1 (en)

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Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4638084A (en) 1985-09-12 1987-01-20 Shell Oil Company Process for dimerizing acrylates and methacrylates
US4889949A (en) 1986-03-27 1989-12-26 Rhone-Poulenc Chimie Catalytic (co)dimerization of alkyl acrylates
EP1070454A1 (de) 1999-02-05 2001-01-24 Suntory Limited Transgenes tier mit gefäss-spezifischer expression des angiotensin-ii2-rezeptors.
WO2008119693A1 (en) 2007-04-03 2008-10-09 Basf Se Dopo flame retardant compositions
JP2013018942A (ja) * 2011-07-14 2013-01-31 Unitika Ltd 難燃性ポリエステル樹脂
US20130136911A1 (en) 2011-11-24 2013-05-30 Ems-Patent Ag Flame-retardant polymer fibres and use thereof and textile fabric comprising these polymer fibres
WO2013139877A1 (de) 2012-03-22 2013-09-26 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Phosphorhaltige ungesättigte polyester, polyesterharze und ggf. faserverstärkte bauteile daraus
CN104211954A (zh) 2013-05-30 2014-12-17 辽宁银珠化纺集团有限公司 一种无卤阻燃尼龙66聚合物的制备方法
CN104231262A (zh) 2014-09-23 2014-12-24 江苏瑞美福实业有限公司 一种有机磷共聚阻燃聚酰胺材料的制备方法
WO2015007783A1 (de) 2013-07-16 2015-01-22 Deutsche Institute Für Textil- Und Faserforschung Denkendorf Verfahren zur herstellung von flammgeschützten copolyamiden, die danach erhältlichen polyamidgarne sowie deren verwendung
WO2018197173A1 (en) 2017-04-25 2018-11-01 Rhodia Operations Flame-retardant polymer; method for preparing it and thermoplastic polymer composition comprising it
CN109180924A (zh) * 2018-09-07 2019-01-11 四川大学 用于水性聚氨酯的反应型氮磷阻燃剂及其制备方法
WO2019081226A1 (en) 2017-10-26 2019-05-02 Rhodia Operations FLAME RETARDANT POLYMER, PROCESS FOR PREPARING THE SAME, AND THERMOPLASTIC POLYMER COMPOSITION COMPRISING THE SAME

Patent Citations (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4638084A (en) 1985-09-12 1987-01-20 Shell Oil Company Process for dimerizing acrylates and methacrylates
US4889949A (en) 1986-03-27 1989-12-26 Rhone-Poulenc Chimie Catalytic (co)dimerization of alkyl acrylates
EP1070454A1 (de) 1999-02-05 2001-01-24 Suntory Limited Transgenes tier mit gefäss-spezifischer expression des angiotensin-ii2-rezeptors.
WO2008119693A1 (en) 2007-04-03 2008-10-09 Basf Se Dopo flame retardant compositions
JP2013018942A (ja) * 2011-07-14 2013-01-31 Unitika Ltd 難燃性ポリエステル樹脂
US20130136911A1 (en) 2011-11-24 2013-05-30 Ems-Patent Ag Flame-retardant polymer fibres and use thereof and textile fabric comprising these polymer fibres
WO2013139877A1 (de) 2012-03-22 2013-09-26 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Phosphorhaltige ungesättigte polyester, polyesterharze und ggf. faserverstärkte bauteile daraus
CN104211954A (zh) 2013-05-30 2014-12-17 辽宁银珠化纺集团有限公司 一种无卤阻燃尼龙66聚合物的制备方法
WO2015007783A1 (de) 2013-07-16 2015-01-22 Deutsche Institute Für Textil- Und Faserforschung Denkendorf Verfahren zur herstellung von flammgeschützten copolyamiden, die danach erhältlichen polyamidgarne sowie deren verwendung
CN104231262A (zh) 2014-09-23 2014-12-24 江苏瑞美福实业有限公司 一种有机磷共聚阻燃聚酰胺材料的制备方法
WO2018197173A1 (en) 2017-04-25 2018-11-01 Rhodia Operations Flame-retardant polymer; method for preparing it and thermoplastic polymer composition comprising it
WO2019081226A1 (en) 2017-10-26 2019-05-02 Rhodia Operations FLAME RETARDANT POLYMER, PROCESS FOR PREPARING THE SAME, AND THERMOPLASTIC POLYMER COMPOSITION COMPRISING THE SAME
CN109180924A (zh) * 2018-09-07 2019-01-11 四川大学 用于水性聚氨酯的反应型氮磷阻燃剂及其制备方法

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
CAS , no. 63562-33-4
D. D. COFFMAN ET AL: "Syntheses by Free-radical Reactions. I. Oxidative Coupling Effected by Hydroxyl Radicals", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 80, no. 11, 1 June 1958 (1958-06-01), US, pages 2864 - 2872, XP055769941, ISSN: 0002-7863, DOI: 10.1021/ja01544a068 *

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